All terms in MONDO
| Label | Id | Description |
|---|---|---|
| Harrod syndrome | MONDO_0010993 | |
| hereditary hemorrhagic telangiectasia type 3 | MONDO_0010996 | |
| microcystic lymphatic malformation | MONDO_0019329 | |
| Charcot-Marie-Tooth disease type 1C | MONDO_0010995 | |
| obsolete isolated vitreoretinopathy | MONDO_0034943 | |
| pemphigus erythematosus | MONDO_0019323 | |
| phakomatosis cesiomarmorata | MONDO_0019326 | |
| phakomatosis cesioflammea | MONDO_0019325 | |
| acanthokeratolytic verrucous nevus | MONDO_0019320 | |
| pemphigus vegetans | MONDO_0019322 | |
| pemphigus vulgaris | MONDO_0008219 | |
| atypical Werner syndrome | MONDO_0019321 | |
| obsolete syndromic ectopia lentis | MONDO_0034937 | |
| dermatocardioskeletal syndrome boronne type | MONDO_0022960 | |
| obsolete colchicine resistance | MONDO_0007348 | |
| desmoplastic infantile astrocytoma | MONDO_0022963 | |
| familial cold autoinflammatory syndrome 1 | MONDO_0007349 | |
| autosomal recessive nonsyndromic hearing loss 8 | MONDO_0010987 | |
| cochleosaccular degeneration-cataract syndrome | MONDO_0007346 | |
| Angelman syndrome due to maternal 15q11q13 deletion | MONDO_0020302 |